Combining Electronic Monitoring With Inhaled Pharmacological Therapy to Manage Cardiac Arrhythmias Including Atrial Fibrillation

ABSTRACT

Disclosed herein are methods of treating cardiac arrhythmia with electronic monitoring in a timely manner. Also disclosed herein are systems for electronic monitoring of cardiac arrhythmia.

CROSS-REFERENCE

This application claims priority to U.S. provisional application No.62/289,473, filed on Feb. 1, 2016, which is herein incorporated byreference in its entirety.

BACKGROUND

The disclosure relates to the use of inhaled CV therapies in combinationwith electronic monitoring devices.

Cardiac arrhythmia (also dysrhythmia) is a term for any of a large andheterogeneous group of conditions in which there can be abnormalelectrical activity in the heart. The heart beat may be too fast or tooslow, and may be regular or irregular.

Cardiac Arrhythmia is a field with a high level of unmet clinical need.Many drugs used today have been on the market since the early 1980s and1990s and are mostly inadequate due to either lack of efficacy or aside-effect profile that can be primarily cardiac related, thatnecessitates extensive monitoring of the subject.

Atrial Fibrillation is a type of Cardiac arrhythmia that occurs as bothsymptomatic and asymptomatic. When symptomatic the subject goes to theER in the hospital for treatment while when asymptomatic that subjectdoes not realize that they are in an arrhythmic state. Atrialfibrillation normally occurs asymptomatically before it becomessymptomatic in short durations. These short episodes spontaneouslyconvert into normal sinus rhythm. But the cumulative effect of theseshort episodes add to the overall AF burden and eventual progression ofthe disease.

Paroxysmal atrial fibrillation (PAF) is a subset of the overall AtrialFibrillation (AF) population and is estimated to be a third of theoverall AF population. AF affects about 34 million people worldwide and11.3 million of these people worldwide are diagnosed as subjects withPAF.

Arrhythmias frequently result in emergency room (ER) visits, whereintravenous drugs are administered, and sometimes necessitating extendedstay in hospital and in some cases also leading to unplanned invasiveprocedures.

Ablation can be expensive and can be about 50% efficacious. Despite thehigh expense, ablation may not completely correct the arrhythmia. Often,multiple ablation procedures are required to achieve a satisfactoryresult in a subject's lifetime. Ablation also results in heart relatedmedical complications associated with morbidity and mortality.

Electronic Monitoring systems are used in subjects to monitor if theyare experiencing such arrhythmias and when an arrhythmia is sustainedthey are recorded and the treating physician is able to assess thecourse of therapy.

What is needed for slowing the progression of AF from its startingparoxysmal state to permanent AF.

None of the current oral or IV approved drug products are combined withan electronic monitoring system with the goal to terminate thearrhythmia at initiation thereby reducing the progression of thedisease, the overall AF burden leading to significant reduction in theeconomies of hospital costs.

Exemplary monitoring devices include the AliveCor Mobile ECG, the RevealLINQ Insertable Cardiac Monitor, the iRhythm ZIO XT Patch, theHeartCheck pen, the AfibAlert, smartphone or portable music playerapplications designed to detect arrhythmias, the Microlife AFIBTechnology device, the WatchBP device, Holter monitors, Smart watches,wearable technology such as those that can vibrate as a means to detectan arrhythmia, or any other similar devices.

SUMMARY

Disclosed herein are methods of treating cardiac arrhythmia in asubject, comprising: (a) identifying cardiac arrhythmia in the subjectwith the aid of an electronic monitoring device; (b) aerosolizing apharmaceutical composition in less than about 9 minutes using aninhaler, wherein the pharmaceutical composition can comprise of atherapeutically effective amount of at least one antiarrhythmic or apharmaceutically acceptable salt thereof; and (c) administering theaerosolized pharmaceutical composition to the subject; thereby treatingthe cardiac arrhythmia. In some embodiments, the identifying of (a)includes an establishing of a duration of the cardiac arrhythmia. Insome embodiments, the duration of the cardiac arrhythmia can be at leastabout 2 hours. In some embodiments, the duration of the cardiacarrhythmia can be at least about 1 hour. In some embodiments, theduration of the cardiac arrhythmia can be at least about 0.5 hours. Insome embodiments, the aerosolizing of the pharmaceutical compositionoccurs in less than 6 minutes. In some embodiments, the aerosolizing ofthe pharmaceutical composition occurs in less than 3 minutes. In someembodiments, the therapeutically effective amount can be an amountsufficient to convert the arrhythmia to normal sinus rhythm. In someembodiments, the therapeutically effective amount can be at least about60 mg of the at least one antiarrhythmic or a pharmaceuticallyacceptable salt thereof In some embodiments, the therapeuticallyeffective amount can be at least about 50 mg of the at least oneantiarrhythmic or a pharmaceutically acceptable salt thereof. In someembodiments, the therapeutically effective amount can be at least about40 mg of the at least one antiarrhythmic or a pharmaceuticallyacceptable salt thereof. In some embodiments, the therapeuticallyeffective amount can be at least about 30 mg of the at least oneantiarrhythmic or a pharmaceutically acceptable salt thereof. In someembodiments, the therapeutically effective amount converts thearrhythmia to normal sinus rhythm from about 0 secs to about 2 hoursafter the administration. In some embodiments, the therapeuticallyeffective amount converts the arrhythmia to normal sinus rhythm in about60 mins after administration. In some embodiments, the treating occurswithin about 120 minutes from an onset of the cardiac arrhythmia. Insome embodiments, the treating occurs within about 90 minutes from anonset of the cardiac arrhythmia. In some embodiments, the treatingoccurs within about 60 minutes from an onset of the cardiac arrhythmia.In some embodiments, the administering can comprise inhalation. In someembodiments, prior to (a), an electronic monitoring chip can be insertedinto the subject. In some embodiments, an electronic monitoring chip canbe worn by the subject. In some embodiments, the electronic monitoringchip can be in communication with the electronic monitoring device. Insome embodiments, the communication can be a wireless communication. Insome embodiments, prior to (a), an electronic monitoring chip can beinserted into the electronic monitoring device. In some embodiments, theidentifying of (a) can comprise a communication of a result to thesubject. In some embodiments, the communication can comprise aninstruction to administer the pharmaceutical composition. In someembodiments, the instruction to administer can comprise a dosage of theaerosolized pharmaceutical composition to administer. In someembodiments, the administering can be performed by the subject. In someembodiments, the administering can be performed by a healthcareprofessional. In some embodiments, the healthcare professional canoverride a recommendation made by the electronic monitoring device. Insome embodiments, the electronic monitoring device waits for aconfirmation from the healthcare provider prior to allowing theadministering of the aerosolized pharmaceutical composition to thesubject. In some embodiments, the communication can comprise making atreatment recommendation. In some embodiments, the treatmentrecommendation can comprise restricting the administration of thepharmaceutical composition when the electronic monitoring device doesnot identify an arrhythmia. In some embodiments, the identifying of (a)can comprise a communication of a result to a healthcare professional.In some embodiments, the administering can be performed by the subject.In some embodiments, the administering can be performed by a healthcareprofessional. In some embodiments, the healthcare professional can be aparamedic. In some embodiments, the healthcare professional can be aphysician. In some embodiments, the healthcare professional can be amonitoring professional. In some embodiments, the healthcareprofessional can override a recommendation made by the electronicmonitoring device. In some embodiments, the electronic monitoring devicewaits for a confirmation from the healthcare provider prior to allowingthe administering of the aerosolized pharmaceutical composition to thesubject. In some embodiments, the communication can comprise making atreatment recommendation. In some embodiments, the treatmentrecommendation can comprise restricting the administration of thepharmaceutical composition when the electronic monitoring device doesnot identify an arrhythmia. In some embodiments, the at least oneantiarrhythmic or salt thereof can be a class I antiarrhythmic. In someembodiments, the class I antiarrhythmic can be a class Ia, Ib, or Icantiarrhythmic. In some embodiments, the class I antiarrhythmic can beflecainide or a salt thereof. In some embodiments, the at least oneantiarrhythmic or salt thereof can be a class II antiarrhythmic. In someembodiments, the at least one antiarrhythmic or salt thereof can be aclass III antiarrhythmic. In some embodiments, the at least oneantiarrhythmic or salt thereof can be a class IV antiarrhythmic. In someembodiments, the at least one antiarrhythmic or salt thereof can be aclass V antiarrhythmic. In some embodiments, the at least oneantiarrhythmic or salt thereof can comprise a sodium channel blocker. Insome embodiments, the at least one antiarrhythmic or salt thereof cancomprise a potassium channel blocker. In some embodiments, the at leastone antiarrhythmic or salt thereof can comprise a calcium channelblocker. In some embodiments, the at least one antiarrhythmic or saltthereof can be rapidly absorbed through a subject's lungs. In someembodiments, the at least one antiarrhythmic or salt thereof can bedelivered to a subject's heart after being absorbed through thesubject's lungs. In some embodiments, the inhaler can be incommunication with the electronic monitoring device. In someembodiments, the communication can be a wired communication. In someembodiments, the communication can be a wireless communication. In someembodiments, the administering of the aerosolized pharmacologicalcomposition by the inhaler can be communicated to the electronicmonitoring device. In some embodiments, the electronic monitoring deviceverifies the administering of the aerosolized pharmaceuticalcomposition. In some embodiments, the electronic monitoring devicecontinues monitoring the progress of the arrhythmia after theadministration. In some embodiments, a recommendation to stop theadministering can be communicated by the electronic monitoring devicewhen the arrhythmia can be converted to a normal sinus rhythm. In someembodiments, a recommendation to seek medical attention can becommunicated by the electronic monitoring device when the arrhythmia canbe not responding to the administration of the pharmaceuticalcomposition as determined by a continued incidence of arrhythmia atleast about 2 hours after the administering. In some embodiments, theelectronic monitoring device can comprise a digital display. In someembodiments, the electronic monitoring device can comprise auditorymeans capable of communicating to the subject. In some embodiments, theelectronic monitoring device can be a smartphone. In some embodiments,the inhaler can comprise a digital display. In some embodiments, theinhaler can comprise auditory means capable of communicating to thesubject.

Also disclosed herein are systems comprising: (a) an electronicmonitoring chip; wherein the electronic monitoring chip monitorsincidence of arrhythmia in a subject; (b) an electronic monitoringdevice; wherein the electronic monitoring device can be in wirelesscommunication with the electronic monitoring chip; and (c) an inhaler;wherein the electronic monitoring device can be in communication withthe inhaler. In some embodiments, the electronic monitoring device canbe in communication with the inhaler through a wired connection. In someembodiments, the electronic monitoring device can be in communicationwith the inhaler through a wireless connection. In some embodiments, theelectronic monitoring device can comprise a digital display. In someembodiments, the electronic monitoring device can comprise auditorymeans capable of communicating to the subject. In some embodiments, theelectronic monitoring device can be a smartphone. In some embodiments,the electronic monitoring chip can be inserted into the subject. In someembodiments, the electronic monitoring chip can be worn by the subject.In some embodiments, the inhaler can comprise a digital display. In someembodiments, the inhaler can comprise auditory means capable ofcommunicating to the subject. In some embodiments, the electronicmonitoring device can comprise storage means. In some embodiments,subject data can be stored using the storage means. In some embodiments,the storage means can be a hard drive. In some embodiments, the storagemeans can be a cloud based storage.

INCORPORATION BY REFERENCE

All publications, patents, and patent applications mentioned in thisspecification are herein incorporated by reference to the same extent asif each individual publication, patent, or patent application wasspecifically and individually indicated to be incorporated by reference.

BRIEF DESCRIPTION OF THE DRAWINGS

The novel features are set forth with particularity in the appendedclaims. A better understanding of features and advantages will beobtained by reference to the following detailed description that setsforth illustrative embodiments, in which exemplary principles areutilized, and the accompanying drawings of which:

FIG. 1 depicts plots of the arterial and venous concentration offlecainide after intravenous or intra-tracheal administration.

FIG. 2 depicts an exemplary physiologically based pharmacokinetic (PBPK)model of the intravenous or intra-tracheal administration of flecainide.

FIG. 3 depicts a plot of the effect on left atrial conduction time afteradministration via intravenous injection or inhalation.

FIG. 4 depicts a plot of the effect of administration of flecainide on asubject's mean blood pressure after administration via intravenousinjection or inhalation.

FIG. 5 depicts a plot of the effect of administration of flecainide on asubject's left ventricular pressure after administration via inhalation.

FIG. 6 depicts a plot of the effect of QTcf prolongation afteradministration of flecainide on a subject's left ventricular pressureafter administration via inhalation.

FIG. 7 depicts an exemplary plot of sinus rhythm using a smart phone asa novel electronic monitoring device as compared to a Prucka System II.

FIG. 8 depicts an exemplary plot of Atrial Fibrillation using a smartphone as a novel electronic monitoring device as compared to a PruckaSystem II.

FIG. 9 depicts an exemplary plot of a treatment of Atrial Fibrillationwith flecainide using a smart phone as a novel electronic monitoringdevice as compared to a Prucka System II.

FIG. 10 depicts an exemplary smart phone application allowing thesmartphone to be used as an electronic monitoring device

FIG. 11 depicts a smart phone in use as an electronic monitoring deviceto monitor treatment of Atrial Fibrillation with flecainide.

DETAILED DESCRIPTION

The details of one or more inventive embodiments are set forth in theaccompanying drawings, the claims, and the description herein. Otherfeatures, objects, and advantages of the inventive embodiments disclosedand contemplated herein can be combined with any other embodiment unlessexplicitly excluded.

Accordingly, disclosed herein are compositions and methods for treatinga heart arrhythmia comprising combining the treatment with an electronicmonitoring system. Other features and advantages will be set forth inthe description that follows, and in part will be apparent from thedescription or may be learned by practice of exemplary embodiments. Thedisclosure will be realized and attained by the compositions and methodsparticularly pointed out in the written description and claims thereof

In some embodiments, the method can be directed to effective monitoringof subjects with AF through electronic means. In some cases, anelectronic monitor can have an ability to record with a subjectinterface to an alert center. In some cases, an electronic monitor canhave an ability to transmit with a subject interface to an alert center.In some cases, an electronic monitor can have an ability to record andtransmit with a subject interface to an alert center. In some cases, anelectronic monitor can have an ability to record without a subjectinterface to an alert center. In some cases, an electronic monitor canhave an ability to transmit without a subject interface to an alertcenter. In some cases, an electronic monitor can have an ability torecord and transmit without a subject interface to an alert center.

In some embodiments, the method can comprise physicians and/or qualifiedpersonnel reading the alert signals from subjects. In some cases, themethod can comprise providing a subject with timely advice toself-administer CV medications to terminate an arrhythmia.

In some embodiments, the method can be directed to effectively shortenthe time of arrhythmia, irrespective of whether it is symptomatic orasymptomatic, by a system where the subject monitoring compliments withthe therapeutic administration of an antiarrhythmic. In some cases, thearrhythmia can be symptomatic. In some cases, the arrhythmia can beasymptomatic

The present invention is directed to an electronic monitoring systemthat is either inserted or is subject enabled combined with a inhalationtherapy that is self-administered either by advise from a monitoringcenter authorized medical personnel or by self-diagnosis of thearrhythmia.

The present invention is directed to administering by inhalation aneffective amount of at least one antiarrhythmic agent to a subject inneed thereof, wherein a cardiac score from a monitor implementing anarrhythmia detection algorithm is detected early in its onset and thesubject's ability to self-administer the inhaled medication to enable atransition from an arrhythmic state to normal sinus rhythm in thesubject within 0 seconds to 2 hours after completion of administration.

Unless otherwise indicated, some embodiments herein contemplatenumerical ranges. When a numerical range is provided, unless otherwiseindicated, the range includes the range endpoints. Unless otherwiseindicated, numerical ranges include all values and sub ranges therein asif explicitly written out.

The singular forms “a”, “an”, and “the” can be used herein to includeplural references unless the context clearly dictates otherwise.Accordingly, unless the contrary is indicated, the numerical parametersset forth in this application can be approximations that may varydepending upon the desired properties sought to be obtained by thepresent invention.

As used herein, the term “salt” is intended to include, but not belimited to, pharmaceutically acceptable salts. And the term“pharmaceutically acceptable salt” is intended to mean those salts thatretain one or more of the biological activities and properties of thefree acids and bases and that are not biologically or otherwiseundesirable. Illustrative examples of pharmaceutically acceptable saltsinclude, but are not limited to, sulfates, pyrosulfates, bisulfates,sulfites, bisulfites, phosphates, monohydrogenphosphates,dihydrogenphosphates, metaphosphates, pyrophosphates, chlorides,bromides, iodides, acetates, propionates, decanoates, caprylates,acrylates, formates, isobutyrates, caproates, heptanoates, propiolates,oxalates, malonates, succinates, suberates, sebacates, fumarates,maleates, butyne-1,4-dioates, hexyne-1,6-dioates, benzoates,chlorobenzoates, methylbenzoates, dinitrobenzoates, hydroxybenzoates,methoxybenzoates, phthalates, sulfonates, xylenesulfonates,phenylacetates, phenylpropionates, phenylbutyrates, citrates, lactates,y-hydroxybutyrates, glycolates, tartrates, methanesulfonates,propanesulfonates, naphthalene-1-sulfonates, naphthalene-2-sulfonates,and mandelates. The term “pharmaceutically acceptable” is intended toinclude, but not be limited to, mean that a component is notbiologically or otherwise undesirable, e.g., the component may beincorporated into a pharmaceutical composition of the invention andadministered to a subject as described herein without causing anysignificant undesirable biological effects or interacting in adeleterious manner with any of the other components of the compositionin which it is contained. When the term “pharmaceutically acceptable” isused to refer to an excipient, it is generally implied that thecomponent has met the required standards of toxicological andmanufacturing testing or that it is included on the Inactive IngredientGuide prepared by the U.S. Food and Drug Administration.

Unless otherwise indicated, “aerosolizing a pharmaceutical composition”means at least about 90% by weight of the pharmaceutical composition isaerosolized. For example, “aerosolizing a pharmaceutical composition inless than 3 minutes” means at least 90% by weight of the pharmaceuticalcomposition is aerosolized in less than 3 minutes.

Unless otherwise indicated, open terms for example “contain,”“containing,” “include,” “including,” and the like mean comprising.

Reference herein to “one embodiment,” “one version,” or “one aspect”shall include one or more such embodiments, versions or aspects, unlessotherwise clear from the context.

As used herein, “tachycardia” means an arrhythmia in which the heartbeat is too fast.

As used herein, the phrase “heart rhythm arrhythmia” means an arrhythmiain which the heart beat is irregular.

As used herein, the “amount of the at least one antiarrhythmic agent inblood in the coronary sinus of the heart” may be measured by extractinga sample from the coronary sinus of the heart by using a cannula. Theamount of antiarrhythmic agent in the sample may then be determined byknown means, such as bioanalytical techniques that employ analyticalequipment such as LC-MS/MS. Thus, the amount of antiarrhythmic agent inthe blood in the heart may be determined for any particular time.

As used herein, the terms “treating” and “treatment” refer to reductionin severity and/or frequency of symptoms, elimination of symptoms and/orunderlying cause, reduction in likelihood of the occurrence of symptomsand/or underlying cause, and/or remediation of damage. Thus, “treating”a subject with an active agent as provided herein includes prevention ofa particular condition, disease, or disorder in a susceptible individualas well as treatment of a clinically symptomatic individual.

As used herein, “nominal amount” refers to the amount contained withinthe unit dose receptacle(s) that can be administered.

As used herein, “effective amount” refers to an amount covering boththerapeutically effective amounts and prophylactically effectiveamounts.

As used herein, a “therapeutically effective amount” of an active agentrefers to an amount that is effective to achieve a desired therapeuticresult. A therapeutically effective amount of a given active agent willtypically vary with respect to factors such as the type and severity ofthe disorder or disease being treated and the age, gender, and weight ofthe subject.

Unless otherwise specified, the term “therapeutically effective amount”includes a “prophylactically effective amount,” i.e., an amount ofactive agent that is effective to prevent the onset or recurrence ofparticular condition, disease, or disorder in a susceptible individual.

Pharmaceutical Composition

In some embodiments, a composition can comprise an antiarrhythmic agent.Examples of antiarrhythmic agents include, but are not limited to, classIa (sodium channel blockers, intermediate association/dissociation),class Ib (sodium channel blockers, fast association/dissociation), classIc (sodium channel blocker, slow association/dissociation), class II(beta blockers), class III (potassium channel blockers), class IV(calcium channel blockers), and class V (unknown mechanisms)antiarrhythmics.

Class Ia antiarrhythmics include, but are not limited to, quinidine,procainamide, and disopyramide. Class Ib antiarrhythmics include, butare not limited to, lidocaine, tocamide, phenyloin, moricizine, andmexiletine. Class Ic antiarrhythmics include, but are not limited to,flecainide, ajmaline, propafenone, and moricizine. Class IIantiarrhythmics include, but are not limited to, propranolol,acebutolol, soltalol, esmolol, timolol, metoprolol, and atenolol. ClassIII antiarrhythmics include, but are not limited to, amiodarone,sotalol, bretylium, ibutilide, E-4031 (methanesulfonamide), vemakalant,and dofetilide. Class IV antiarrhythmics include, but are not limitedto, bepridil, nitrendipine, amlodipine, isradipine, nifedipine,nicardipine, verapamil, and diltiazem. Class V antiarrhythmics include,but are not limited to, digoxin and adenosine.

The pharmaceutical composition can also include derivatives of the aboveantiarrhythmic pharmaceutical agents such as solvates, salts (e.g.,acetate), solvated salts, esters, amides, hydrazides, N-alkyls, and/orN-amino acyls. In some cases, the pharmaceutical composition is a liquidpharmaceutical composition. Examples of ester derivatives include, butare not limited to, methyl esters, choline esters, anddimethylaminopropyl esters. Examples of amide derivatives include, butare not limited to, primary, secondary, and tertiary amides. Examples ofhydrazide derivatives include, but are not limited to,N-methylpiperazine hydrazides. Examples of N-alkyl derivatives include,but are not limited to, N′,N′,N′-trimethyl and N′,N′-dimethylaminopropylsuccininimidyl derivatives of antiarrhythmic pharmaceutical agent methylesters. Examples of N-aminoacyl derivatives include, but are not limitedto, N-omithyl-, N-diaminopropionyl-, N-lysil-, N-hexamethyllysil-, andN-piperidine-propionyl- orN′,N′-methyl-l-piperazine-propionyl-antiarrhythmic pharmaceutical agentmethyl esters.

The pharmaceutical composition can comprise one or more antiarrhythmicpharmaceutical agents and, optionally, one or more pharmaceuticallyacceptable excipients. The pharmaceutically acceptable excipient cancomprise lipids, metal ions, surfactants, amino acids, carbohydrates,buffers, salts, polymers, and the like, and combinations thereof. Insome cases, the pharmaceutically acceptable excipient is water. In somecases, the pharmaceutically acceptable excipient is not water. Examplesof lipids include, but are not limited to, phospholipids, glycolipids,ganglioside GMI, sphingomyelin, phosphatidic acid, cardiolipin; lipidsbearing polymer chains such as polyethylene glycol, chitin, hyaluronicacid, or polyvinylpyrrolidone; lipids bearing sulfonated mono-, di-, andpolysaccharides; fatty acids such as palmitic acid, stearic acid, andoleic acid; cholesterol, cholesterol esters, and cholesterolhemisuccinate. The pharmaceutically acceptable excipient can compriseone or more osmolality adjuster, such as sodium chloride. For instance,sodium chloride may be added to solutions to adjust the osmolality ofthe solution. In one or more embodiments, an aqueous compositionconsists essentially of the antiarrhythmic pharmaceutical agent, theosmolality adjuster, and water. The pharmaceutically acceptable can alsocomprise a buffer or a pH adjusting agent, typically a salt preparedfrom an organic acid or base. For example, the pharmaceuticalcompositions typically have a pH ranging from 3.5 to 8.0, such as from4.0 to 7.5, 4.5 to 7.0, or 5.0 to 6.5. Representative buffers compriseorganic acid salts of citric acid, lactic acid, ascorbic acid, gluconicacid, carbonic acid, tartaric acid, succinic acid, acetic acid, orphthalic acid, tris, trimethamine hydrochloride, or phosphate buffers.Thus, the buffers include citrates, phosphates, phthalates, andlactates. It may be desirable to add other pharmaceutically acceptableexcipients to the pharmaceutical composition to improve particlerigidity, production yield, emitted dose and deposition, shelf-life, andsubject acceptance. Such optional pharmaceutically acceptable excipientsinclude, but are not limited to: coloring agents, taste masking agents,buffers, hygroscopic agents, antioxidants, and chemical stabilizers.

As noted above, the pharmaceutical composition may include one or moresurfactants. For instance, one or more surfactants may be in the liquidphase with one or more being associated with (e.g., the pharmaceuticalcompositions may incorporate, adsorb, absorb, be coated with, or beformed by the surfactant) solid particles or particles of thecomposition. By “associated with” it is meant that the pharmaceuticalcompositions may incorporate, adsorb, absorb, be coated with, or beformed by the surfactant. Surfactants include, but are not limited to,fluorinated and nonfluorinated compounds, such as saturated andunsaturated lipids, nonionic detergents, nonionic block copolymers,ionic surfactants, and combinations thereof. Examples of ionicsurfactants include, but are not limited to, sodium sulfosuccinate, andfatty acid soaps. Examples of buffers include, but are not limited to,tris or citrate. Examples of acids include, but are not limited to,carboxylic acids. Examples of carbohydrates include, but are not limitedto, monosaccharides, disaccharides, and polysaccharides. For example,monosaccharides such as dextrose (e.g. anhydrous and monohydrate),galactose, mannitol, D-mannose, sorbitol, sorbose and the like;disaccharides such as lactose, maltose, sucrose, trehalose, and thelike; trisaccharides such as raffinose and the like; and othercarbohydrates such as starches (e.g., hydroxyethyl starch),cyclodextrins, and maltodextrins.

The pharmaceutical composition can comprise one or more antiarrhythmicpharmaceutical agents and, can include one or more additional activeagents, for example, agents that may be delivered through the lungs.Additional active agents may comprise, for example, hypnotics andsedatives, psychic energizers, tranquilizers, respiratory drugs,anticonvulsants, muscle relaxants, anti-Parkinson agents (e.g. dopamineantagonists), analgesics, anti-inflammatories, antianxiety drugs (e.g.anxiolytics), appetite suppressants, antimigraine agents, musclecontractants, additional anti-infectives (e.g. antivirals, antifungals,vaccines) antiarthritics, antimalarials, antiemetics, anepileptics,cytokines, growth factors, anti-cancer agents, antithrombotic agents,antihypertensives, cardiovascular drugs, antiarrhythmics, antioxidants,anti-asthma agents, hormonal agents including contraceptives,sympathomimetics, diuretics, lipid regulating agents, antiandrogenicagents, antiparasitics, anticoagulants, neoplastics, antineoplastics,hypoglycemics, nutritional agents and supplements, growth supplements,antienteritis agents, vaccines, antibodies, diagnostic agents, andcontrasting agents. The additional active agent, when administered byinhalation (e.g., as an aerosol), may act locally or systemically.

The amount of antiarrhythmic pharmaceutical agent in the pharmaceuticalcomposition can vary. The amount of antiarrhythmic pharmaceuticalagent(s) can be about 0.1% to 100% by weight of the total amount of thepharmaceutical composition. In some cases, the amount of antiarrhythmicpharmaceutical agent(s) is at least about 0.1% by weight of the totalamount of the pharmaceutical composition, for example, at least about0.1%, 0.2%, 0.3%, 0.4%, 0.5%, 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%,15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%,85%, 90%, 95%, or 100% by weight of the total amount of thepharmaceutical composition. In some cases, the amount of antiarrhythmicpharmaceutical agent(s) is about 0.1%-100% by weight of the total amountof the pharmaceutical composition, for example, about 0.1%-1%, 0.1%-5%,0.1-10%, 0.1%-20%, 0.5%-1%, 0.5%-5%, 0.5%-10%, 0.5%-20%, 1%-5%, 1%-10%,1%-20%, 5%-10%, 5%-20%, 10%-20%, 10%-30%, 20%-30%, 20%-40%, 30%-40%,30%-50%, 40%-50%, 40%-60%, 50%-60%, 50%-70%, 60%-70%, 60%-80%, 70%-80%,70%-90%, 80%-90%, 80%-95%, 90%-95%, 90%-99%, 90%-100%, 95%-99%, or99%-100% by weight of the total amount of the pharmaceuticalcomposition.

Method of Treatment

Described herein are methods of treating a condition in a subjectpharmaceutical comprising delivering a pharmaceutical compositiondisclosed herein. The condition can be cardiac arrhythmia including, butnot limited to, tachycardia, supraventricular, tachycardia (SVT),paroxysmal supraventricular tachycardia (PSVT), atrial fibrillation(AF), paroxysmal atrial fibrillation (PAF), permanent atrialfibrillation, persistent atrial fibrillation, atrial flutter, paroxysmalatrial flutter, and lone atrial fibrillation.

One aspect of embodiments disclosed herein is the surprising andunexpected rate at which the antiarrhythmic agents pass through theheart. While a skilled artisan might expect the rate to be too fast,modeling and empirical evidence indicates that the drug will not passthrough the heart too fast. Thus, a therapeutic effect is achieveddespite fast pass-through and despite only one pass-through attherapeutic levels

Also described are methods to treat acute episodes of and/or chronicarrhythmias. In certain embodiments, the treating can comprise acutetreatment after detection of cardiac arrhythmia.

Flecainide can be effective via IV at doses of 75-150 mg administered ina hospital or other suitable medical facility. The equilibration betweenarterial concentration and venous concentration can occur rapidly. Onthe other hand, inhalation can target the drug to the pulmonary veinthat originates in the lung capillaries, and the left atrium where PAForiginates. Inhalation can be started much earlier at onset rather thanthe subject waiting to go to the hospital for an IV. Alternatively,Flecainide can be also administered orally as a bolus of 300 mg (max perday) dose at one time to terminate PAF. Via this route, it can take anaverage of 100 minutes to terminate the PAF. Oral flecainide is 30-50%effective. Subjects who take this maximum dose are restricted until 24hours to take any further antiarrhythmics. Conversely, an inhalationdose can be several orders of magnitude less than the oral dose, andthus permit repeat doses of flecainide.

The method of treatment via inhalation can result in a pulsatilepharmacokinetic profile and transient pharmacodynamic effect mimickingthe effect of an IV. The method can delivers high drug concentrationsthat are safe and effective to the heart, while the distribution to therest of the body results in the drug being diluted to sub-therapeuticlevels. This method is the shortest route of delivery to the heart nextto intracardial injection. This provides the convenience ofself-administration like the “pill-in-the-pocket” approach, but theeffectiveness and fast onset of action of an IV. Although the deliveryof medications through the lung for systemic effect is not new, it waswidely thought it wouldn't be effective to the heart, because of thefast passage of the drug through it, not having time to act on thetarget tissue. The PK/PD modeling and empirical evidence originatingthis invention shows that the drug exposure is sufficient fortherapeutic effect at a much lower dose compared to other routes ofadministration. This method ensures dug concentrations in overall plasmaare much lower than what is achieved by oral/IV hence minimizingdrug-drug interactions and side effects.

The subject can be a mammal in need thereof, preferably such mammal is ahuman subject. Examples of subjects include, but are not limited to,pediatric subjects, adult subjects, and geriatric subjects. In someembodiments, the pharmaceutical composition is intended only as atreatment for rapid resolution of symptoms and is not taken as apreventative, i.e., when the subject is well, there is no need fordrug-this makes the therapy more effective and safe due to sporadic orintermittent dosing, and focused on reducing disabling symptoms.

Unit doses of the pharmaceutical compositions may be contained in acontainer. Examples of containers include, but are not limited to,syringes, capsules, blow fill seal, blisters, vials, ampoules, bottles,or container closure systems made of metal, polymer (e.g., plastic,elastomer), glass, or the like. For instance, the vial may be acolorless Type I borosilicate glass ISO 6R 10 mL vial with a chlorobutylrubber siliconized stopper, and rip-off type aluminum cap with coloredplastic cover.

The unit dose can comprise at least about 0.1 mL of the pharmaceuticalcomposition, for example, at least about 0.1, 0.2, 0.3, 0.4, 0.5, 0.6,0.7, 0.8, 0.9, 1, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6, 6.5, 7, 7.5,8, 8.5, 9, 9.5, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 25, 30, 35,40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, or 100 mL of thepharmaceutical composition. The unit dose can comprise about 0.1-100 mLof the pharmaceutical composition, for example, about 0.1-0.2, 0.1-0.5,0.1-1.0, 0.2-0.5, 0.2-1.0, 0.5-1.0, 0.5-1.5, 0.5-2.0, 0.5-3.0, 0.5-4.0,0.5-5.0, 1.0-2.0, 1.0-3.0, 1.0-4.0, 1.0-5.0, 2.0-3.0, 2.0-4.0, 2.0-5.0,3.0-5.0, 5-10, 10-20, 20-30, 30-40, 40-50, 50-60, 60-70, 70-80, 80-90,or 90-100 mL of the pharmaceutical composition. In some cases, the unitdose of the pharmaceutical composition ranges from about 2 ml to about15 ml, such as from about 3 ml to about 10 ml, about 4 ml to about 8 ml,or about 5 ml to about 6 ml.

The container may be inserted into an aerosolization device (e.g.,inhaler). The container may be of a suitable shape, size, and materialto contain the pharmaceutical composition and to provide thepharmaceutical composition in a usable condition.

The compositions of the present invention may be made by any of thevarious methods and techniques known and available to those skilled inthe art. For instance, a solution of antiarrhythmic pharmaceutical agentmay be made using the following procedure. Typically, manufacturingequipment is sterilized before use. A portion of the final volume, e.g.,70%, of solvent, e.g., water for injection, may be added into a suitablecontainer. Antiarrhythmic pharmaceutical agent may then be added. Theantiarrhythmic pharmaceutical agent may be mixed until dissolved.Additional solvent may be added to make up the final batch volume. Thebatch may be filtered, e.g., through a 0.2 μm filter into a sterilizedreceiving vessel. Filling components may be sterilized before use infilling the batch into vials, e.g., 10 ml vials. As an example, theabove-noted sterilizing may include the following. A 5 liter type 1glass bottle and lid may be placed in an autoclave bag and sterilized atelevated temperature, e.g., 121° C., for 15 minutes, using an autoclave.Similarly, vials may be placed into suitable racks, inserted into anautoclave bag, and sterilized at elevated temperature, e.g., 121° C.,for 15 minutes, using an autoclave. Also similarly, stoppers may beplaced in an autoclave bag and sterilized at elevated temperature, e.g.,121° C., for 15 minutes, using an autoclave. Before sterilization,sterilizing filters may be attached to tubing, e.g., a 2 mm length of 7mm×13 mm silicone tubing. A filling line may be prepared by placed in anautoclave bag and sterilized at elevated temperature, e.g., 121° C., for15 minutes, using an autoclave. Sterilization may also be accomplishedusing electronic beams or gamma rays. The filling may also be conductedunder laminar flow protection. The filling line may be unwrapped andplaced into the receiving bottle. The sterilized vials and stoppers maybe unwrapped under laminar flow protection. Each vial may be filled,e.g., to a target fill of 5 g, and stoppered. A flip off collar may beapplied to each vial. The sealed vials may be inspected for vialleakage, correct overseals, and cracks.

As another example, an antiarrhythmic may be prepared by lyophilizingthe antiarrhythmic to form a powder for storage. The powder is thenreconstituted prior to use. This technique may be used when theantiarrhythmic is unstable in solution. The solvent for the solution tobe lyophilized may comprise water. The solution may be excipient-free.For instance, the solution may be cryoprotectant-free. In one or moreembodiments, a suitable amount (e.g., 30 mg per mL of final solution) ofdrug substance may be dissolved, e.g., in about the 75% of thetheoretical total amount of water for injection under nitrogen bubbling.The dissolution time may be recorded and appearance may be evaluated.Then, the dilution to the final volume with water for injection (WFI)may be carried out. Final volume may be checked. Density, pH, endotoxin,bioburden, and content by UV may be measured both before and aftersterile filtration.

The solution may be filtered before lyophilizing. For instance, a double0.2 μm filtration may be performed before filling. The filters may betested for integrity and bubble point before and after the filtration.Pre-washed and autoclaved vials may be aseptically filled using anautomatic filling line to a target of 5 ml per vial and then partiallystoppered. In process check for fill volumes may be done by checking thefill weight every 15 minutes. The lyophilizing is generally conductedwithin about 72 hours, such as within about 8 hours, or within about 4hours, of the dissolving. In one or more embodiments, the lyophilizingcan comprise freezing the solution to form a frozen solution. The frozensolution is typically held at an initial temperature ranging from about−40° C. to about −50° C., such as about −45° C. During the initialtemperature period, the pressure around the frozen solution is typicallyatmospheric pressure. The initial temperature period typically rangesfrom about 1 hour to about 4 hours, such about 1.5 hours to about 3hours, or about 2 hours. The lyophilizing may further comprise raising atemperature of the frozen solution to a first predetermined temperature,which may range from about 10° C. to about 20° C., such as about 15° C.The time for the heat ramp from the initial temperature to the firstpredetermined temperature generally ranges from about 6 hours to about10 hours, such as about 7 hours to about 9 hours. During the firstpredetermined temperature period, the pressure around the solutiontypically ranges from about 100 μbar to about 250 μbar, such as about150 μbar to about 225 μbar. The solution may be held at the firstpredetermined temperature for a period ranging from about 20 hours toabout 30 hours, such as from about 24 hours. The lyophilizing may stillfurther comprise raising a temperature of the solution to a secondpredetermined temperature, which may range from about 25° C. to about35° C., such as about 30° C. During the second predetermined temperatureperiod, the pressure around the frozen solution typically ranges fromabout 100 μbar to about 250 μbar, such as about 150 μbar to about 225μbar. The solution may be held at the second predetermined temperaturefor a period ranging from about 10 hours to about 20 hours.

The lyophilization cycle may comprise a freezing ramp, e.g., from 20° C.to −45° C. in 65 minutes, followed by a freeze soak, e.g., at −45° C.for 2 hours. Primary drying may be accomplished with a heating ramp,e.g., from −45° C. to 15° C. in 8 hours, followed by a temperature hold,e.g., at 15° C. for 24 hours at a pressure of 200 μbar. Secondary dryingmay be accomplished with a heating ramp, e.g., from 15° C. to 30° C. in15 minutes, followed by a temperature hold at 30° C. for 15 hours at apressure of 200 μbar. At the end of the lyophilization cycle, the vacuummay be broken with sterile nitrogen, and the vials may be automaticallystoppered. The water content of the lyophilized powder is typically lessthan about 7 wt %, such as less than about 5 wt %, less than about 4 wt%, less than about 3 wt %, less than about 2 wt %, or less than about 1wt %. The powder is capable of being reconstituted with water at 25° C.and 1.0 atmosphere and with manual agitation, in less than about 60seconds, such as less than about 30 seconds, less than about 15 seconds,or less than about 10 seconds. The powder typically has a large specificsurface area that facilitates reconstitution. The specific surface areatypically ranges from about 5 m²/g to 20 m²/g, such as about 8 m²/g to15 m²/g, or about 10 m²/g to 12 m²/g. Upon reconstitution with water,the antiarrhythmic pharmaceutical agent solution typically has a pH thatranges from about 2.5 to about 7, such as about 3 to about 6.

The compositions of one or more embodiments of the present invention maybe administered by inhalation. Moreover, the doses of composition thatare inhaled can be much less than those administered by other routes andrequired to obtain similar effects. It may be due to the efficienttargeting of the inhaled composition to the heart.

The dosage necessary and the frequency of dosing of the antiarrhythmicpharmaceutical agent depend on the composition and concentration of theantiarrhythmic pharmaceutical agent within the composition. In somecases, the dose is less than its normal intravenous dose. The pulmonarydose can be similar to intracardial doses.

Inhalation avoids the initial dilution of drug in the body as comparedto intravenous or oral dosing. Inhalation also avoids first-passmetabolism, such as hepatic metabolism. For instance, calcium channelblockers, such as diltiazem, undergo significant hepatic metabolism whentaken orally. Inhalation allows rapid delivery of the parent diltiazemcompound to the heart as a bolus. Surprisingly, administration byinhalation of diltiazem via the inhalation route according to thepresent invention converted atrial fibrillation to normal sinus rhythmand reduced heart rate. Thus, administration by inhalation of diltiazemis useful for treating both atrial fibrillation and supraventriculartachycardia (SVT). In contrast, administration by IV of diltiazem istypically only used for converting SVT to normal sinus rhythm and inatrial fibrillation to reduce heart rate (not for converting to normalsinus rhythm). Inhalation also avoids red blood cell metabolism. Forinstance, the reduced dilution and short route associated withinhalation reduces red blood cell metabolism of esmolol. Inhalation mayalso avoid reduced blood pressure and fainting. For instance, IVadministration of beta blockers, such as esmolol, and/or Class Iantiarrhythmics such as flecainide, may reduce mean arterial bloodpressure (MAP). Inhalation can allow rapid delivery of esmolol and/orflecainide without reducing MAP. As a result, inhalation of betablockers and/or Class I antiarrhythmics may result in an MAP of 10 mm Hgto 20 mm Hg greater than the MAP resulting from IV administration of thesame beta blocker or Class I antiarrhythmic. With inhaled cardiotherapythe drug is directed to the heart from the lungs as a bolus. So, theheart sees a high concentration. The drug is rapidly diluted as itpasses through the heart, but the exposure time is sufficient for thedesired pharmacological action. Once the drug passes through the heart,the concentration of the drug in the overall blood is below thetherapeutic concentration and is considered ineffective and thus safer.The therapeutic window is the range of dosage of a drug or of itsconcentration in a bodily system that provides safe effective therapy.Anything below the minimum amount is sub-therapeutic and henceineffective in that concentration. In view of the dilution, unwantedside effects are minimized.

The dose may be administered during a single inhalation or may beadministered during several inhalations. The fluctuations ofantiarrhythmic pharmaceutical agent concentration can be reduced byadministering the pharmaceutical composition more often or may beincreased by administering the pharmaceutical composition less often.Therefore, the pharmaceutical composition of one or more embodiments ofthe present invention may be administered from about four times daily toabout once a month, such as about once daily to about once every twoweeks, about once every two days to about once a week, and about onceper week. The pharmaceutical composition can also be administered to thesubject on an as-needed basis.

In some cases, the pharmaceutical composition in accordance with one ormore embodiments of the invention may be administered from about 1 toabout 4 times daily, such as from about 2 to about 3 times daily. Insome cases, the antiarrhythmic may be administered daily. In some cases,the administration can be at least about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10,11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28,29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46,47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, or 62 timesa month.

In some cases, an antiarrhythmic pharmaceutical agent or salt thereofcan be administered at a dose of from about 1 mg to about 480 mg, fromabout 5 mg to about 480 mg, from about 10 mg to about 480 mg, from about15 mg to about 480 mg, from about 20 mg to about 480 mg, from about 25mg to about 480 mg, from about 30 mg to about 480 mg, from about 35 mgto about 480 mg, from about 40 mg to about 480 mg, from about 45 mg toabout 480 mg, from about 50 mg to about 480 mg, from about 55 mg toabout 480 mg, from about 60 mg to about 480 mg, from about 65 mg toabout 480 mg, from about 70 mg to about 480 mg, from about 75 mg toabout 480 mg, from about 80 mg to about 480 mg, from about 85 mg toabout 480 mg, from about 90 mg to about 480 mg, from about 95 mg toabout 480 mg, from about 100 mg to about 480 mg, from about 105 mg toabout 480 mg, from about 110 mg to about 480 mg, from about 115 mg toabout 480 mg, from about 120 mg to about 480 mg, from about 125 mg toabout 480 mg, from about 130 mg to about 480 mg, from about 135 mg toabout 480 mg, from about 140 mg to about 480 mg, from about 145 mg toabout 480 mg, from about 150 mg to about 480 mg, from about 155 mg toabout 480 mg, from about 160 mg to about 480 mg, from about 165 mg toabout 480 mg, from about 170 mg to about 480 mg, from about 175 mg toabout 480 mg, from about 180 mg to about 480 mg, from about 185 mg toabout 480 mg, from about 190 mg to about 480 mg, from about 195 mg toabout 480 mg, from about 200 mg to about 480 mg, from about 205 mg toabout 480 mg, from about 210 mg to about 480 mg, from about 215 mg toabout 480 mg, from about 220 mg to about 480 mg, from about 225 mg toabout 480 mg, from about 230 mg to about 480 mg, from about 235 mg toabout 480 mg, from about 240 mg to about 480 mg, from about 245 mg toabout 480 mg, from about 250 mg to about 480 mg, from about 255 mg toabout 480 mg, from about 260 mg to about 480 mg, from about 265 mg toabout 480 mg, from about 270 mg to about 480 mg, from about 275 mg toabout 480 mg, from about 280 mg to about 480 mg, from about 285 mg toabout 480 mg, from about 290 mg to about 480 mg, from about 295 mg toabout 480 mg, or from about 300 mg to about 480 mg.

In some cases, an antiarrhythmic pharmaceutical agent or salt thereofdescribed herein can be administered at a dose of about 1, 2, 3, 4, 5,6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24,25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42,43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60,61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78,79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96,97, 98, 99, 100, 101, 102, 103, 104, 105, 106, 107, 108, 109, 110, 111,112, 113, 114, 115, 116, 117, 118, 119, 120, 121, 122, 123, 124, 125,126, 127, 128, 129, 130, 131, 132, 133, 134, 135, 136, 137, 138, 139,140, 141, 142, 143, 144, 145, 146, 147, 148, 149, 150, 151, 152, 153,154, 155, 156, 157, 158, 159, 160, 161, 162, 163, 164, 165, 166, 167,168, 169, 170, 171, 172, 173, 174, 175, 176, 177, 178, 179 180, 181,182, 183, 184, 184, 186, 187, 188, 189, 190, 191, 192, 193, 194, 195,196, 197, 198, 199, 200, 201, 202, 203, 204, 205, 206, 207, 208, 209,210, 211, 212, 213, 214, 215, 216, 217, 218, 219, 220, 221, 222, 223,224, 225, 226, 227, 228, 229, 230, 231, 232, 233, 234, 235, 236, 237,238, 239, 240, 242, 243, 244, 245, 246, 247, 248, 249. 250, 251, 252,253, 254, 255, 256, 257, 258, 259, 260, 261, 262, 263, 264, 265, 266,267, 268, 269, 270, 271, 272, 273, 274, 275, 276, 277, 278, 279, 280,281, 282, 283, 284, 285, 286, 287, 288, 289, 290, 291, 292, 293, 294,295, 296, 297, 298, 299, 300, 301, 302, 303, 304, 305, 306, 307, 308,309, 310, 311, 312, 313, 314, 315, 316, 317, 318, 319, 320, 321, 322,323, 324, 325, 326, 327, 328, 329, 330, 331, 332, 333, 334, 335, 336,337, 338, 339, 340, 341, 342, 343, 344, 345, 346, 347, 348, 349, 350,351, 352, 353, 354, 355, 356, 357, 358, 359, 360, 361, 362, 363, 364,365, 366, 367, 368, 369,370, 371, 372, 373, 374, 375, 376, 377, 378,379, 380, 381, 382, 383, 384, 385, 386, 387, 388, 389, 390, 391, 392,393, 394, 395, 396, 397, 398, 399, 400, 401, 402, 403, 404, 405, 406,407, 408, 409, 410, 411, 412, 413, 414, 415, 416, 417, 418, 419, 420,421, 422, 423, 424, 425, 426, 427, 428, 429, 430, 431, 432, 433, 434,435, 436, 437, 438, 439, 440, 441, 442, 443, 444, 445, 446, 447, 448,449, 450, 451, 452, 453, 454, 455, 456, 457, 458, 459, 460, 461, 462,463, 464, 465, 466, 467, 468, 469, 470, 471, 472, 473, 474, 475, 476,477, 478, 479, or 480 mg.

In some exemplary embodiments, a daily dosage of an antiarrhythmicpharmaceutical agent (e.g. flecainide) can range from about 0.1 mg toabout 600 mg, such as about 0.5 mg to about 500 mg, about 1 mg to about400 mg, about 2 mg to about 300 mg, and about 3 mg to about 200 mg.

For treating a subject suffering from arrhythmia, the amount per dose ofantiarrhythmic pharmaceutical agent (e.g. flecainide) administered maybe an amount that is effective to treat the arrhythmia. The amount ofantiarrhythmic pharmaceutical agent (e.g. flecainide) for the treatmentof arrhythmia can be at least about 0.001 mg/kg, such as at least about0.001 mg/kg, 0.002 mg/kg, 0.003 mg/kg, 0.004 mg/kg, 0.005 mg/kg, 0.01mg/kg, 0.02 mg/kg, 0.04 mg/kg, 0.06 mg/kg, 0.08 mg/kg, 0.1 mg/kg, 0.2mg/kg, 0.3 mg/kg, 0.4 mg/kg, 0.5 mg/kg, 0.6 mg/kg, 0.7 mg/kg, 0.8 mg/kg,0.9 mg/kg, 1 mg/kg, 1.5 mg/kg, 2 mg/kg, 2.5 mg/kg, 3 mg/kg, 3.5 mg/kg, 4mg/kg, 4.5 mg/kg, 5 mg/kg, or 6 mg/kg. The amount of antiarrhythmicpharmaceutical agent (e.g. flecainide) for the treatment of arrhythmiacan range from about 0.001 mg/kg to 6 mg/kg, such as from about 0.001mg/kg to about 0.01 mg/kg, from about 0.01 mg/kg to about 0.05 mg/kg,from about 0.05 mg/kg to about 0.1 mg/kg, from about 0.1 mg/kg to about0.2 mg/kg, from about 0.1 mg/kg to about 0.5 mg/kg, from about 0.1 mg/kgto about 1 mg/kg, from about 0.1 mg/kg to about 2 mg/kg, from about 0.1mg/kg to about 3 mg/kg, from about 0.3 mg/kg to about 1 mg/kg, fromabout 0.3 mg/kg to about 2 mg/kg, from about 0.3 mg/kg to about 3 mg/kg,from about 0.5 mg/kg to about 1 mg/kg, from about 0.5 mg/kg to about 2mg/kg, from about 0.5 mg/kg to about 3 mg/kg, from about 0.5 mg/kg toabout 6 mg/kg, from about 0.7 mg/kg to about 1 mg/kg, from about 0.7mg/kg to about 2 mg/kg, from about 0.7 mg/kg to about 4 mg/kg, fromabout 0.7 mg/kg to about 6 mg/kg, from about 1 mg/kg to about 2 mg/kg,from about 1 mg/kg to about 4 mg/kg, from about 1 mg/kg to about 6mg/kg, from about 2 mg/kg to about 3 mg/kg, from about 2 mg/kg to about4 mg/kg, from about 2 mg/kg to about 6 mg/kg, or from about 3 mg/kg toabout 6 mg/kg.

The amount of antiarrhythmic pharmaceutical agent (e.g. flecainide) forthe treatment of arrhythmia can be at least about 0.1 mg, such as atleast about 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1, 1.5, 2, 2.5,3, 3.5, 4, 4.5, 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9, 9.5, 10, 11, 12, 13,14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 30, 35, 40, 45, 50, 60,70, 80, 90, 100, 110, 120, 130, 140, or 150 mg. The amount ofantiarrhythmic pharmaceutical agent (e.g. flecainide) for the treatmentof arrhythmia can range about 0.01-150 mg, such as about 0.1-150,0.1-130, 0.1-110, 0.1-90, 0.1-70, 0.1-50, 0.1-30, 0.1-10, 0.1-5,0.1-1.0, 0.1-0.5, 1-150, 1-130, 1-110, 1-90, 1-70, 1-50, 1-30, 1-10,1-5, 5-150, 5-130, 5-110, 5-90, 5-70, 5-50, 5-30, 5-10, 10-150, 10-130,10-110, 10-90, 10-70, 10-50, 10-30, 30-150, 30-130, 30-110, 30-90,30-70, 30-50, 50-150, 50-130, 50-110, 50-90, 50-70, 70-150, 70-130,70-110, 70-90, 90-150, 90-130, 90-110, 110-150, 110-130, or 130-150 mg.For example, the amount of antiarrhythmic pharmaceutical agent (e.g.flecainide) for the treatment of arrhythmia can range about from 0.1 toabout 5 mg.

In some instances, an antiarrhythmic can be administered as a unit dose.In some cases, a unit dose can be a dose of from about 0.1 mg to about100 mg or greater of an antiarrhythmic pharmaceutical agent to the lungin a single inhalation. The above described phospholipid hollow and/orporous dry powder particles allow for doses of about 5 mg or greater,often greater than about 10 mg, sometimes greater than about 15 mg,sometimes greater than about 20 mg, sometimes greater than about 25 mg,sometimes greater than about 30 mg, sometimes greater than about 35 mg,sometimes greater than about 40 mg, sometimes greater than about 45 mg,sometimes greater than about 50 mg, sometimes greater than about 55 mg,sometimes greater than about 60 mg, sometimes greater than about 65 mg,sometimes greater than about 70 mg, sometimes greater than about 75 mg,sometimes greater than about 80 mg, sometimes greater than about 85 mg,sometimes greater than about 90 mg, sometimes greater than about 95 mg,or sometimes greater than about 100 mg, to be delivered in a singleinhalation and in an advantageous manner. Alternatively, a dosage may bedelivered over two or more inhalations, such as at least 2, 3, 4, 5, 6,7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 25, 30, 35, 40, 45,50, 55, 60, 65, 70, 75, 80, 85, 90, 95 or 100 inhalations. A dosage mayalso be delivered over 1 to 100 inhalations, such as 1-3, 1-4, 1-5, 1-6,1-10, 1-20, 1-50, 1-80, 1-100, 2-5, 2-6, 2-10, 2-20, 2-50, 2-100, 5-10,5-20, 5-50, 5-100, 10-20, 10-50, 10-100, 20-50, 20-100, or 50-100inhalations. For example, a 10 mg dosage may be delivered by providingtwo unit doses of 5 mg each, and the two unit doses may be separatelyinhaled. In certain embodiments, the overall dose of the antiarrhythmicpharmaceutical agent ranges from 0.1 mg to 200 mg, such as 0.5 mg to 150mg, or 1 mg to 100 mg. In some instances the antiarrhythmic agent can beadministered as-needed titrating the dosage to effect.

The concentration of antiarrhythmic pharmaceutical agent (e.g.flecainide) for the treatment of arrhythmia can be at least about 0.1mg/mL, such as at least about 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8,0.9, 1, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9,9.5, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 25, 30, 35, 40, 45, 50,55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 110, 120, 130, 140, or 150mg/mL. For example, the concentration of antiarrhythmic pharmaceuticalagent (e.g. flecainide) for the treatment of arrhythmia can be at leastabout 30 mg/mL in an acetate buffer. The concentration of antiarrhythmicpharmaceutical agent (e.g. flecainide) for the treatment of arrhythmiacan range about 0.1-150 mg/mL, such as about 0.1-130, 0.1-110, 0.1-90,0.1-70, 0.1-50, 0.1-30, 0.1-10, 0.1-5, 0.1-1.0, 0.1-0.5, 1-150, 1-130,1-110, 1-90, 1-70, 1-50, 1-30, 1-10, 1-5, 5-150, 5-130, 5-110, 5-90,5-70, 5-50, 5-30, 5-10, 10-150, 10-130, 10-110, 10-90, 10-70, 10-50,10-30, 30-150, 30-130, 30-110, 30-90, 30-70, 30-50, 50-150, 50-130,50-110, 50-90, 50-70, 70-150, 70-130, 70-110, 70-90, 90-150, 90-130,90-110, 110-150, 110-130, or 130-150 mg/mL. For example, theconcentration of antiarrhythmic pharmaceutical agent (e.g. flecainide)for the treatment of arrhythmia can range about 30-50 mg/mL in anacetate buffer.

The present invention can be directed to a method of self-diagnosing andtreating cardiac arrhythmia. The method can comprise self-diagnosingcardiac arrhythmia by detecting at least one of shortness of breath,heart palpitations, and above normal heart rate. The method also cancomprise self-administering by inhalation an effective amount of atleast one antiarrhythmic pharmaceutical agent within two hours, such aswithin one hour, 30 minutes, or within 15 minutes, of theself-diagnosing. In some cases, the subject can self-titrate. Forexample, the subject can self-administer, e.g., by using an inhaler,until disabling symptoms disappear. In some cases, theself-administering continues until the subject no longer feels heartpalpitations.

The time for onset of action is also typically short. For instance, thesubject may have normal sinus rhythm within 20 minutes of initiating theadministering, such as within 15 minutes, within 10 minutes, or within 5minutes of initiating the administering. The rapid onset of action isadvantageous because the longer a subject has had arrhythmia, the longerit typically takes to convert the subject to normal sinus rhythm. Insome embodiments, the method of the present invention allows the subjectto avoid other therapies, such as ablation and/or electricalcardioversion. In other embodiments, the method of the present inventionis used in combination with other therapies, such as before or afterelectrical cardioversion and/or ablation therapy.

Device

The pharmaceutical composition may be delivered by an inhaler asdescribed in WO 99116420, by a metered dose inhaler as described in WO99116422, by a liquid dose instillation apparatus as described in WO99116421. Inhalers impart energy into a liquid pharmaceuticalcomposition to aerosolize the liquid, and to allow delivery to thepulmonary system, e.g., the lungs, of a subject. An inhaler can comprisea liquid delivery system, such as a container having a reservoir thatcontains a liquid pharmaceutical composition. The liquid pharmaceuticalcomposition generally can comprise an active agent that is either insolution or suspended within a liquid medium.

In one type of inhaler, generally referred to as a jet inhaler,compressed gas is forced through an orifice in the container. Thecompressed gas forces liquid to be withdrawn through a nozzle, and thewithdrawn liquid mixes with the flowing gas to form aerosol droplets. Acloud of droplets is then administered to the subject's respiratorytract. The compressed gas can be compressed air or compressed oxygen.

In another type of inhaler, generally referred to as a vibrating meshinhaler, energy, such as mechanical energy, vibrates a mesh. Thisvibration of the mesh aerosolizes the liquid pharmaceutical compositionto create an aerosol cloud that is administered to the subject's lungs.The vibrating mesh inhaler can comprise a metal vibrating mesh. In somecases, iron constitutes at least about 30% weight, such as 30%, 40%,50%, 60%, 70%, 80%, or 90% of the metal vibrating mesh. An inhaler ofthe vibrating mesh type, such as one that that forms droplets withoutthe use of compressed gas, such as the Aeroneb® Pro can provideunexpected improvement in dosing efficiency and consistency. Bygenerating fine droplets by using a vibrating perforated or unperforatedmembrane, rather than by introducing compressed air, the aerosolizedpharmaceutical formulation can be introduced without substantiallyaffecting the flow characteristics. In addition, the generated dropletswhen using an inhaler of this type are introduced at a low velocity,thereby decreasing the likelihood of the droplets being driven to anundesired region.

In still another type of inhaler, generally referred to as an ultrasonicwave inhaler, ultrasonic waves or ultrasonic agitations are generated todirectly vibrate and aerosolize the pharmaceutical formulation.

Alternatively or additionally, the pharmaceutical composition may be ina liquid form and may be aerosolized using an inhaler as described in WO2004/071368, which is herein incorporated by reference in its entirety,as well as U.S. Published application Nos. 2004/0011358 and2004/0035413, which are both herein incorporated by reference in theirentireties. Other examples of inhalers include, but are not limited to,the Aeroneb Go or Aeroneb® Pro nebulizers, available from Aerogen Ltd.of Galway, Ireland; the PARI eFlow and other PARI nebulizers availablefrom PARI Respiratory Equipment, Inc. of Midlothian, Va.; the Lumiscope®Nebulizer 6600 or 6610 available from Lumiscope Company, Inc. of EastBrunswick, N.J.; and the Omron NE-U22 available from Omron Healthcare,Inc. of Kyoto, Japan.

The inhaler has the ability to rapidly deliver the aerosol at a ratethat assures availability of a bolus dose in the heart. The inhaler canaerosolize the pharmaceutical composition in short amount of time. Insome cases, the inhaler can aerosolize the pharmaceutical composition(e.g. at least 30 mg of flecainide) in less than about 20 minutes, suchas less than about 10 seconds, 20 seconds, 30 seconds, 1 minute, 2minutes, 3 minutes, 4 minutes, 5 minutes, 6 minutes, 7 minutes, 8minutes, 9 minutes, 10 minutes, 11 minutes, 12 minutes, 13 minutes, 14minutes, 15 minutes, 16 minutes, 17 minutes, 18 minutes, 19 minutes, or20 minutes. For example, the inhaler can aerosolize at least 30 mg offlecainide in less than 3 minutes. In some cases, the inhaler canaerosolize the pharmaceutical composition in about 10 seconds to 20minutes, such as about 10-20 seconds, 10-30 seconds, 10 seconds to 1minute, 10 seconds to 2 minute, 10 seconds to 3 minute, 20-30 seconds,20 seconds to 1 minute, 20 seconds to 2 minute, 20 seconds to 3 minute,30 seconds to 1 minute, 30 seconds to 2 minutes, 30 seconds to 3minutes, 1-2 minutes, 1-5 minutes, 2-20 minutes, 2-10 minutes, 2-5minutes, 5-20 minutes, 5-10 minutes, or 10-20 minutes. For example, theinhaler can aerosolize at least 30 mg of flecainide in about 30 secondsto 3 minutes.

One or more embodiments of the present invention may be used inconjunction with liquid dose instillation or LDI techniques as disclosedin, for example, WO 99116421, which is incorporated herein by referencein its entirety. Liquid dose instillation involves the directadministration of a formulation to the lung. With respect to LDI theformulations are preferably used in conjunction with partial liquidventilation or total liquid ventilation. Moreover, one or moreembodiments of the present invention may further comprise introducing atherapeutically beneficial amount of a physiologically acceptable gas(such as nitric oxide or oxygen) into the pharmaceuticalmicro-dispersion prior to, during or following administration.

The pharmaceutical composition of one or more embodiments of the presentinvention typically has improved emitted dose efficiency. Accordingly,high doses of the pharmaceutical composition may be delivered using avariety of aerosolization devices and techniques. The emitted dose (ED)of the particles of the present invention may be greater than about 30%,such as greater than about 40%, greater than about 50%, greater thanabout 60%, or greater than about 70%.

The present invention may involve a follow-up inhalation if nocardioversion occurs after an initial inhalation. Typically, if nocardioversion occurs within 30 minutes of the initial inhalation, thefollow-up dosage is higher or the same as the initial dosage. The dosingmay be guided by how the subject feels.

Electronic Systems

In some cases, an electronic system can be used to monitor an occurrenceor incidence of atrial fibrillation, and administer treatment to asubject in need thereof. Exemplary embodiments of a system can includean electronic monitoring chip, an electronic monitoring device, and aninhaler. Each component of a system can be in communication with any orall components of the system. The terms “communication,” “communicated,”“in communication with,” “transmission,” and “receiving” can refer toelectronic exchange or communication between devices. In some instances,the exchange can occur though a wired connection between the devicessuch as through the use of a USB cord or fiber optic connection. In someinstances, the exchange can occur through a wireless connection betweenthe devices. In some cases, a wireless signal can be sent through amobile data network such as a 4G LTE or 3G data signal. In some cases, awireless signal can be sent through a Bluetooth connection. In somecases, a wireless signal can be sent through a Wi-Fi connection. In somecases, a wireless signal can be sent through an infra-red dataassociation link.

An electronic monitoring chip can be inserted or implanted into asubject, and be used to detect a signal that correlates to an ECG in thesubject. Alternatively, or in addition to insertion, an electronicmonitoring chip can be worn by a subject. In some cases, an electronicmonitoring device can be a component of a wearable electronic devicesuch as a watch, ankle bracelet, and the like. An electronic monitoringchip can be in communication with an electronic monitoring device, aninhaler, or both. In some exemplary embodiments, a communication can bea wireless communication.

An electronic monitoring device may include but not limited to hand heldheart monitors, hand held ECG monitors, Bluetooth App-Enabled Monitors,and the like. In some cases, a smartphone can be used as an electronicmonitoring device. Such a device can include an application that canallow a smartphone to communicate with a that have the ability totransmit the cardiac readings to a monitoring center and/or chips andloop recorders inserted into a subject for the purpose of diagnosis andpharmacological intervention.

In some cases, an electronic monitoring device can include means toinstruct a subject, or other personnel. In some cases, an audiblesource, a tactile source, and/or a visual source can be included. Insome cases, an audible source can be a device producing sound. In someembodiments an audible source can be one or more speakers. A tactilesource can comprise a tactile sensor. In some embodiments, a tactilesensor can detect a stimuli resulting from mechanical stimulation, ortemperature. A visual source can be a light, multiple lights, gauge,display or the like. For example, in an exemplary embodiment the visualsource can be a screen on a handheld device.

In some cases, an inhaler as described herein can be employed as part ofa system. In some instances, the inhaler can be in communication with anelectronic monitoring system. An electronic monitoring system can beused to direct administration of a pharmaceutical composition by aninhaler in communication therewith. In some cases, an electronic devicecan allow administration of the pharmaceutical composition by theinhaler. For example, an electronic device may allow administration whenan electronic monitoring chip detects an incidence of atrialfibrillation. In some cases, an electronic device can preventadministration of the pharmaceutical composition by the inhaler. Forexample, an electronic device may prevent administration when anelectronic monitoring chip does not detect an incidence of atrialfibrillation; when a healthcare professional overrides anadministration; or when administration is deemed unsafe.

In some cases, an inhaler can contain visual, audible, or tactilesources as described above.

Furthermore, a system described herein can perform self-monitoringchecks to detect and alert of potential fault conditions.

In some instances, dosing may be guided by a portable ECG. For instance,the dosing may be guided by a heart monitoring device (e.g. Holtermonitor). In another version, the pharmaceutical composition isadministered prophylactically to a subject who is likely to develop anarrhythmia. For example, a subject who has a history of arrhythmias canbe prophylactically treated with a pharmaceutical composition comprisingantiarrhythmic pharmaceutical agent to reduce the likelihood ofdeveloping an arrhythmia. The pharmaceutical composition may beadministered to a subject in any regimen which is effective to preventan arrhythmia. Illustrative prophylactic regimes include administeringan antiarrhythmic pharmaceutical agent as described herein 1 to 21 timesper week. In some cases, an overall cumulative arrhythmic burden iscontrolled by monitoring.

In some cases, a result can be communicated to a healthcare profession.A healthcare professional can include a physician, a paramedic, a nurse,and the like. A system or device herein can be employed by a healthcareprofessional in a number of settings, including, but not limited to, ahospital, hospice, clinic, office, ambulance, nursing home, and thelike. In some cases, a result can be communicated to a non-healthcareprofessional. In some cases, a result can be communicated to amonitoring center. In some instances, a monitoring center can contactthe subject between 0 secs to 60 mins for the purpose of communicatingthe diagnosis and ascertaining the subject's ability to self-administerthe dose of the inhaled antiarrhythmic.

Employment of a system described herein can produce an overallmanagement of arrhythmia. This can result in fewer hospital visits, ERvisits and extended hospitalizations.

In some cases, a system or component thereof can be capable ofcommunicating with doctors, health providers, health providerorganizations or their computerized systems to notify that thearrhythmia has been detected, the doses and nature of thepharmacological agent delivered, and the response of the arrhythmia tothe pharmacological dose.

A method can comprise administering to free breathing subjects by way ofan aerosol generator device and/or system for administration ofaerosolized medicaments such as those disclosed in U.S. PublishedApplication Nos. 20050235987, 20050211253, 20050211245, 20040035413, and20040011358, the disclosures of which are incorporated herein byreference in their entireties.

Also disclosed herein are kits for treating cardiac arrhythmias. Forinstance, the kit may include an aerosolization device and/or acontainer, e.g., unit dose receptacle, containing aerosolizableantiarrhythmic pharmaceutical agent (e.g., flecainide), for example, asa liquid or dry powder. The kit may further comprise a package, such asa bag, that contains the aerosolization device and/or the container. Thekit may further comprise instructions for the aerosolization deviceand/or the container.

EXAMPLES Example 1: Evaluation of Rate of Aerosolization in DifferentBuffer and Solution Systems

The methods disclosed herein relate to the nebulization of flecainideacetate solution for treating AF, PAF and PSVT, e.g. when they manifestas acute episodes. It can be essential that the inhaler has the abilityto rapidly deliver the aerosol at a rate that assures availability of abolus dose in the heart. When a pharmaceutical composition of flecainidearound 30-40 mg/mL in an acetate buffer is used, one would require 1 to2.0 ml of the drug to be dosed within 1-3 minutes to be effective.

The time required for aerosolizing solutions with different buffer andexcipient systems were tested and measured using an Omron MicroAirdevice (Table 1). The aerosolization time for aerosolizing 0.3 mL ofeach solution was recorded. The device used was a vibrating mesh that ismade of a Titanium-nickel alloy.

TABLE 1 Evaluation of rate of aerosolization in different buffer andsolution systems using the Omron MicroAir Aerosolization Rate time (s)(mL/ Sample (0.3 mL) min) 0.9% sodium 27 0.67 chloride (control) 30 mMacetate 34 0.53 22.5 mM acetate 27 0.67 15 mM acetate 30 0.60 7.5 mMacetate 31 0.58 40 mg/mL solution 281 0.06 30 mg/mL solution 260 0.07 20mg/mL solution 213 0.08 10 mg/mL solution 131 0.14 40 mg/mL solution 2810.06 30 mg/mL solution 224 0.08 (22.5 mM acetate) 20 mg/mL solution 1820.10 (15 mM acetate) 10 mg/mL solution 134 0.13 (7.5 mM acetate)

Example 2: Assessment of Different Inhalers with Flecainide Acetate (FA)Solution

Different inhalers were then tested to assess compatibility of materialto the different materials of construction and different types ofinhalers (Table 2).

TABLE 2 Assessment of different inhalers with flecainide acetate (FA)solution at 30 mg/ml. Device Material of Average St dev Device Typeconstruction Solution (mL/min) (mL/min) Voyager Vi- Not known 30 mg/mLFA 0.16 0.01 brating Saline 0.29 0.01 AeroNeb Mesh Nickel- 30 mg/mL FA0.06 0.01 Solo Palladium Saline 0.55 0.01 Pari Stainless 30 mg/mL FA0.61 0.06 eRapid steel Saline 0.84 0.09 Mini- Ultra- No mesh 30 mg/mL FA0.13 0.04 Breeze sonic Saline 0.29 0.02 Lumi- 30 mg/mL FA 0.85 0.03scope Saline 1.08 0.07 CompXP Com- 30 mg/mL FA 0.14 0.02 pressed Saline0.14 0.01 Trek S air 30 mg/mL FA 0.34 0.01 (PART) Saline 0.26 0.01

The above results showed that a 30-40 mg dose of flecainide can beeffectively delivered using the Pari e-rapid or Lumiscope inhalers inless than 2 minutes. The Trek S from PARI was able to deliver the samedose in about 3 minutes.

Example 3: Assessment of Flecainide Acetate (FA) Efficacy using anElectronic Monitoring System

An exemplary smart phone app was installed on a smartphone in order tomonitor the efficacy of FA at ceasing incidence of atrial fibrillation.The smartphone app allowed for communication between the smart phone andan electronic monitoring chip used to produce an ECG.

FIG. 7 depicts an exemplary ECG produced from a smartphone as comparedto a Prucka System in an animal in sinus rhythm. The traces showexcellent correlation between the two devices.

FIG. 8 depicts an exemplary ECG produced from a smartphone as comparedto a Prucka System in an animal displaying atrial fibrillation. Again,the traces show excellent correlation between the two devices.

The smart phone device was then used to monitor the treatment efficacyof an intra-tracheal administration of 0.75 mg/kg flecainide in treatingatrial fibrillation. FIG. 9 depicts an exemplary ECG produced from asmartphone as compared to a Prucka System in an animal displaying atrialfibrillation. Again, the traces show excellent correlation between thetwo devices. Each device shows a return to sinus rhythm uponadministration. FIG. 10 depicts the actual employment of the smart phoneto monitor the return to sinus rhythm in the animal. FIG. 12 depicts acomparison of the animal before and after administration of flecainideusing the smartphone, which again showed a conversion back to sinusrhythm in the animal.

While preferred embodiments of the present invention have been shown anddescribed herein, it will be obvious to those skilled in the art thatsuch embodiments are provided by way of example only. Numerousvariations, changes, and substitutions will now occur to those skilledin the art without departing from the invention. It should be understoodthat various alternatives to the embodiments of the invention describedherein may be employed in practicing the invention. It is intended thatthe following claims define the scope of the invention and that methodsand structures within the scope of these claims and their equivalents becovered thereby.

What is claimed is: 1-82. (canceled)
 83. A method of treating cardiacarrhythmia in a subject, comprising: (a) receiving an instruction foradministering an aerosolized pharmaceutical composition from anelectronic monitoring device; and (b) administering said aerosolizedpharmaceutical composition from an aerosolization device to said subjectaccording to said instruction, wherein said aerosolized pharmaceuticalcomposition comprises a therapeutically effective amount of at least oneantiarrhythmic or a pharmaceutically acceptable salt thereof
 84. Themethod of claim 83, wherein said administering comprises inhalation. 85.The method of claim 83, wherein said aerosolization device comprises aninhaler.
 86. The method of claim 85, wherein said inhaler is incommunication with said electronic monitoring device.
 87. The method ofclaim 85, wherein said inhaler comprises a digital display.
 88. Themethod of claim 85, wherein said inhaler comprises auditory meanscapable of communicating to said subject.
 89. The method of claim 83,wherein said administering is performed by said subject.
 90. The methodof claim 83, wherein said administering is performed by a healthcareprofessional.
 91. The method of claim 83, wherein said at least oneantiarrhythmic or pharmaceutically acceptable salt thereof is a class Iantiarrhythmic, class II antiarrhythmic, class III antiarrhythmic, classIV antiarrhythmic, class V antiarrhythmic, or a salt of any of these.92. The method of claim 83, wherein said at least one antiarrhythmic orpharmaceutically acceptable salt thereof comprises flecainide acetate.93. The method of claim 83, wherein said electronic monitoring deviceprovides said instruction when identifying said cardiac arrhythmia. 94.The method of claim 93, wherein said identifying comprises establishinga duration of said cardiac arrhythmia.
 95. The method of claim 94,wherein said duration of the cardiac arrhythmia is at least about 0.5hours.
 96. The method of claim 83, wherein said instruction comprisesallowing said administering of said aerosolized pharmaceuticalcomposition when detecting an occurrence of said cardiac arrhythmia. 97.The method of claim 83, wherein said instruction comprises a dosage ofsaid aerosolized pharmaceutical composition to administer.
 98. Themethod of claim 83, wherein said instruction comprises restricting saidadministration of said pharmaceutical composition when said electronicmonitoring device does not identify said cardiac arrhythmia.
 99. Themethod of claim 83, wherein said electronic monitoring device waits fora confirmation from a healthcare provider prior to allowing saidadministering of said aerosolized pharmaceutical composition to saidsubject.
 100. The method of claim 83, wherein said administering of saidaerosolized pharmaceutical composition is communicated to saidelectronic monitoring device.
 101. The method of claim 83, wherein saidelectronic monitoring device verifies said administering of saidaerosolized pharmaceutical composition.
 102. The method of claim 83,wherein said therapeutically effective amount is an amount sufficient toconvert said arrhythmia to normal sinus rhythm.
 103. The method of claim83, wherein said therapeutically effective amount is at least about 30mg of said at least one antiarrhythmic or a pharmaceutically acceptablesalt thereof
 104. The method of claim 83, wherein said therapeuticallyeffective amount converts said arrhythmia to normal sinus rhythm fromabout 0 secs to about 2 hours after said administration.
 105. The methodof claim 83, wherein said electronic monitoring device is incommunication with an electronic monitoring chip that is inserted intosaid subject or worn by said subject.
 106. The method of claim 83,wherein said electronic monitoring device comprises a digital display orauditory means capable of communicating to said subject.
 107. The methodof claim 83, wherein said electronic monitoring device is a smartphone.